Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3013501525

FEI Number

3013501525

Entity Name

COZZIA USA LLC

City/State/Country

Covina, CA, US

Establishment Address

861 S Oak Park Road, Covina, CA 91724, US

Establishment Type(s)

Complaint File Establishment per 21 CFR 820.198

Owner / Operator

Cozzia USA LLC (Owner Number: 10054381)

Owner / Operator Contact Address

861 S Oak Park Road, Covina, CA 91724, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

K95

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
MSH	Respirator, Surgical	General, Plastic Surgery	Class 2	878.4040	2020-03-14

Official Correspondent

George Hattub

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Cozzia USA LLC

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K102092	Prestige Ameritech	PRO GEAR N95 PARTICULATE FILTER RESPIRATOR & SURGICAL MASK, REGULAR SIZE MODEL RP CERIES	2010-10-06

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3041850200	RISKWISE SUPPLIES LLC	Lorton, VA, US
3018382937	MID-AMERICA SAFETY CORP	Elk Grove Village, IL, US
3010141571	Xiantao Zhongyi Safety & Protection Products Co.,Ltd.	Xiantao City Hubei, CN

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3013501525. Last updated year: 2026. Please use registration number 3013501525 when referencing this establishment in official correspondence.